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- Oppenauer_oxidation abstract "Oppenauer oxidation, named after Rupert Viktor Oppenauer, is a gentle method for selectively oxidizing secondary alcohols to ketones.The reaction is the opposite of Meerwein-Ponndorf-Verley reduction. The alcohol is oxidized with aluminium isopropoxide in excess acetone. This shifts the equilibrium toward the product side.The oxidation is highly selective for secondary alcohols and does not oxidize other sensitive functional groups such as amines and sulfides. Though primary alcohols can be oxidized under Oppenauer conditions, primary alcohols are seldom oxidized by this method due to the competing aldol condensation of aldehyde products. The Oppenauer oxidation is still used for the oxidation of acid labile substrates. The method has been largely displaced by oxidation methods based on chromates (e.g. PCC) or dimethyl sulfoxide (e.g. Swern oxidation) or Dess-Martin oxidation due to its use of relatively mild and non-toxic reagents (e.g. the reaction is run in acetone/benzene mixtures). The Oppenanuer oxidation is commonly used in various industrial processes such as the synthesis of steroids, hormones, alkaloids, terpenes, etc.".
- Oppenauer_oxidation thumbnail Oppenauer_oxidation_reaction_scheme.png?width=300.
- Oppenauer_oxidation wikiPageID "6343849".
- Oppenauer_oxidation wikiPageRevisionID "604766400".
- Oppenauer_oxidation hasPhotoCollection Oppenauer_oxidation.
- Oppenauer_oxidation subject Category:Name_reactions.
- Oppenauer_oxidation subject Category:Organic_redox_reactions.
- Oppenauer_oxidation type ChemicalProcess113446390.
- Oppenauer_oxidation type ChemicalReaction113447361.
- Oppenauer_oxidation type NameReactions.
- Oppenauer_oxidation type NaturalProcess113518963.
- Oppenauer_oxidation type OrganicRedoxReactions.
- Oppenauer_oxidation type PhysicalEntity100001930.
- Oppenauer_oxidation type Process100029677.
- Oppenauer_oxidation comment "Oppenauer oxidation, named after Rupert Viktor Oppenauer, is a gentle method for selectively oxidizing secondary alcohols to ketones.The reaction is the opposite of Meerwein-Ponndorf-Verley reduction. The alcohol is oxidized with aluminium isopropoxide in excess acetone. This shifts the equilibrium toward the product side.The oxidation is highly selective for secondary alcohols and does not oxidize other sensitive functional groups such as amines and sulfides.".
- Oppenauer_oxidation label "Oppenauer oxidation".
- Oppenauer_oxidation label "Oppenauer-Oxidation".
- Oppenauer_oxidation label "Oppenauer-oxidatie".
- Oppenauer_oxidation label "Ossidazione di Oppenauer".
- Oppenauer_oxidation label "Oxidación de Oppenauer".
- Oppenauer_oxidation label "Oxydation d'Oppenauer".
- Oppenauer_oxidation label "オッペナウアー酸化".
- Oppenauer_oxidation label "沃氏氧化反应".
- Oppenauer_oxidation sameAs Oppenauer-Oxidation.
- Oppenauer_oxidation sameAs Oxidación_de_Oppenauer.
- Oppenauer_oxidation sameAs Oxydation_d'Oppenauer.
- Oppenauer_oxidation sameAs Ossidazione_di_Oppenauer.
- Oppenauer_oxidation sameAs オッペナウアー酸化.
- Oppenauer_oxidation sameAs Oppenauer-oxidatie.
- Oppenauer_oxidation sameAs m.0g1_rq.
- Oppenauer_oxidation sameAs Q902263.
- Oppenauer_oxidation sameAs Q902263.
- Oppenauer_oxidation sameAs Oppenauer_oxidation.
- Oppenauer_oxidation wasDerivedFrom Oppenauer_oxidation?oldid=604766400.
- Oppenauer_oxidation depiction Oppenauer_oxidation_reaction_scheme.png.
- Oppenauer_oxidation isPrimaryTopicOf Oppenauer_oxidation.